FDA Drug recall D-1224-2014
Black Ant, 4600 mg x 4. Product is packaged in a small green box with gold lettering on the front, the back side of the box contains mostly…
- FDA Drug
- Class I
- terminated
- Published 2014-04-16
On 2014-04-16 the FDA classified a Class I recall of Black Ant, 4600 mg x 4. Product is packaged in a small green box with gold lettering on the front, the back side of the box contains mostly… by American Lifestyle Com, citing marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1224-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-04-30 |
| Published | 2014-04-16 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | American Lifestyle Com |
| Distribution | n/a |
Product
Black Ant, 4600 mg x 4. Product is packaged in a small green box with gold lettering on the front, the back side of the box contains mostly foreign character. Within the box there are four (4) capsules individually wrapped in black and red plastic with white lettering. UPC 4026666142546 (product numbers may possibly vary for same product identification and same product packaging).
Reason
Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains undeclared sildenafil. Tadalafil and sildenafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the Vicerex and the Black Ant products unapproved new drugs.
Identifiers
| upc | 4026666142546 |
|---|---|
| code_info | All lots, UPC 4026666142546. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1224-2014%22
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